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Disease association ontology term - MONDO:0015541 - hereditary hemophagocytic lymphohistiocytosis

Term summary

ID
MONDO:0015541
Name
hereditary hemophagocytic lymphohistiocytosis
Ontology or CV name
Disease association
Definition
An instance of hemophagocytic lymphohistiocytosis that is caused by an inherited genomic modification in an individual.

Parents

Annotation

Disease association

MONDO:0008963 - Chediak-Higashi syndrome

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Genes:

MONDO:0012146 - familial hemophagocytic lymphohistiocytosis 3

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Genes:

MONDO:0011336 - familial hemophagocytic lymphohistiocytosis 4

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Genes:

MONDO:0013135 - familial hemophagocytic lymphohistiocytosis 5

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Genes:

MONDO:0011997 - Hermansky-Pudlak syndrome 2

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Genes: